Canonical Allele Identifier: CA2202017924
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2084953T= , CM000678.2:g.2084953T= GRCh38
NC_000016.9:g.2134954T= , CM000678.1:g.2134954T= GRCh37
NC_000016.8:g.2074955T= NCBI36
NG_005895.1:g.40648T= , LRG_487:g.40648T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2845T= ENSP00000455997.2:n.*2845T=
ENST00000642206.2:c.4343T= ENSP00000495146.2:p.Phe1448=
ENST00000642365.2:c.4493T= ENSP00000495459.2:p.Phe1498=
ENST00000644417.2:c.*4876T= ENSP00000493912.2:n.*4876T=
ENST00000646464.2:c.*7245T= ENSP00000496610.2:n.*7245T=
ENST00000219476.9:c.4496T= MANE Select ENSP00000219476.3:p.Phe1499=
ENST00000350773.9:c.4427T= ENSP00000344383.4:p.Phe1476=
ENST00000401874.7:c.4295T= ENSP00000384468.2:p.Phe1432=
ENST00000568454.6:c.4328T= ENSP00000454487.1:p.Phe1443=
ENST00000569110.2:c.719T=
ENST00000569930.2:n.2378T=
ENST00000642365.1:c.3150T=
ENST00000642561.1:c.4367T= ENSP00000495099.1:p.Phe1456=
ENST00000642728.1:n.678T=
ENST00000642797.1:c.4298T= ENSP00000493846.1:p.Phe1433=
ENST00000642936.1:c.4364T= ENSP00000494514.1:p.Phe1455=
ENST00000643088.1:c.4295T= ENSP00000494747.1:p.Phe1432=
ENST00000643177.1:n.510T=
ENST00000643426.1:n.2144T=
ENST00000643946.1:c.4427T= ENSP00000495927.1:p.Phe1476=
ENST00000644043.1:c.4367T= ENSP00000496262.1:p.Phe1456=
ENST00000644329.1:c.4295T= ENSP00000496611.1:p.Phe1432=
ENST00000644335.1:c.4298T= ENSP00000496317.1:p.Phe1433=
ENST00000644399.1:c.4417T=
ENST00000645024.1:n.2580T=
ENST00000646388.1:c.4496T= ENSP00000495921.1:p.Phe1499=
ENST00000646634.1:n.3311T=
ENST00000646674.1:n.1748T=
ENST00000647042.1:n.1719T=
ENST00000647180.1:n.1609T=
ENST00000219476.7:c.4496T= ENSP00000219476.3:p.Phe1499=
ENST00000350773.8:c.4427T= ENSP00000344383.4:p.Phe1476=
ENST00000382538.10:c.4151T= ENSP00000371978.6:p.Phe1384=
ENST00000401874.6:c.4295T= ENSP00000384468.2:p.Phe1432=
ENST00000439117.6:c.*3663T= ENSP00000406980.2:n.*3663T=
ENST00000439673.6:c.4187T= ENSP00000399232.2:p.Phe1396=
ENST00000497886.5:n.2254T=
ENST00000568454.5:c.4328T= ENSP00000454487.1:p.Phe1443=
ENST00000569110.1:c.678T=
ENST00000569930.1:n.1611T=
NM_000548.3:c.4496T= , LRG_487t1:c.4496T= NP_000539.2:p.Phe1499=
NM_001077183.1:c.4295T= NP_001070651.1:p.Phe1432=
NM_001114382.1:c.4427T= NP_001107854.1:p.Phe1476=
XM_005255529.3:c.4367T= XP_005255586.2:p.Phe1456=
XM_005255531.3:c.4298T= XP_005255588.2:p.Phe1433=
XM_011522636.1:c.4550T= XP_011520938.1:p.Phe1517=
XM_011522637.1:c.4547T= XP_011520939.1:p.Phe1516=
XM_011522638.1:c.4439T= XP_011520940.1:p.Phe1480=
XM_011522639.1:c.4421T= XP_011520941.1:p.Phe1474=
XM_011522640.1:c.4418T= XP_011520942.1:p.Phe1473=
XM_011522641.1:c.4187T= XP_011520943.1:p.Phe1396=
NM_000548.4:c.4496T= NP_000539.2:p.Phe1499=
NM_001077183.2:c.4295T= NP_001070651.1:p.Phe1432=
NM_001114382.2:c.4427T= NP_001107854.1:p.Phe1476=
NM_001318827.1:c.4187T= NP_001305756.1:p.Phe1396=
NM_001318829.1:c.4151T= NP_001305758.1:p.Phe1384=
NM_001318831.1:c.3764T= NP_001305760.1:p.Phe1255=
NM_001318832.1:c.4328T= NP_001305761.1:p.Phe1443=
NM_001363528.1:c.4298T= NP_001350457.1:p.Phe1433=
NM_021055.2:c.4367T= NP_066399.2:p.Phe1456=
XM_005255531.4:c.4298T= XP_005255588.2:p.Phe1433=
XM_011522636.2:c.4550T= XP_011520938.1:p.Phe1517=
XM_011522637.2:c.4547T= XP_011520939.1:p.Phe1516=
XM_011522638.2:c.4712T= XP_011520940.2:p.Phe1571=
XM_011522639.2:c.4421T= XP_011520941.1:p.Phe1474=
XM_011522640.2:c.4418T= XP_011520942.1:p.Phe1473=
XM_017023615.1:c.4493T= XP_016879104.1:p.Phe1498=
XM_017023616.1:c.4364T= XP_016879105.1:p.Phe1455=
XM_017023617.1:c.4460T= XP_016879106.1:p.Phe1487=
XM_017023618.1:c.3206T= XP_016879107.1:p.Phe1069=
XM_024450413.1:c.4295T= XP_024306181.1:p.Phe1432=
NM_000548.5:c.4496T= MANE Select NP_000539.2:p.Phe1499=
NM_001370404.1:c.4364T= NP_001357333.1:p.Phe1455=
NM_001370405.1:c.4367T= NP_001357334.1:p.Phe1456=
NM_001077183.3:c.4295T= NP_001070651.1:p.Phe1432=
NM_001114382.3:c.4427T= NP_001107854.1:p.Phe1476=
NM_001318827.2:c.4187T= NP_001305756.1:p.Phe1396=
NM_001318829.2:c.4151T= NP_001305758.1:p.Phe1384=
NM_001318831.2:c.3764T= NP_001305760.1:p.Phe1255=
NM_001318832.2:c.4328T= NP_001305761.1:p.Phe1443=
NM_001363528.2:c.4298T= NP_001350457.1:p.Phe1433=
NM_021055.3:c.4367T= NP_066399.2:p.Phe1456=